Last synced on 25 April 2025 at 11:05 pm

ViaOne Epicardial Access System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K243928
510(k) Type
Traditional
Applicant
CardioVia Ltd.
Country
Israel
FDA Decision
Substantially Equivalent
Decision Date
3/20/2025
Days to Decision
90 days
Submission Type
Summary

ViaOne Epicardial Access System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K243928
510(k) Type
Traditional
Applicant
CardioVia Ltd.
Country
Israel
FDA Decision
Substantially Equivalent
Decision Date
3/20/2025
Days to Decision
90 days
Submission Type
Summary